Variant STAT4 and Response to Ruxolitinib in an Autoinflammatory Syndrome von Baghdassarian, Hratch, Blackstone, Sarah A., Clay, Owen S., Philips, Rachael, Matthiasardottir, Brynja, Nehrebecky, Michele, Hua, Vivian K., McVicar, Rachael, Liu, Yang, Tucker, Suzanne M., Randazzo, Davide, Deuitch, Natalie, Rosenzweig, Sofia, Mark, Adam, Sasik, Roman, Fisch, Kathleen M., Pimpale Chavan, Pallavi, Eren, Elif, Watts, Norman R., Ma, Chi A., Gadina, Massimo, Schwartz, Daniella M., Sanyal, Anwesha, Werner, Giffin, Murdock, David R., Horita, Nobuyuki, Chowdhury, Shimul, Dimmock, David, Jepsen, Kristen, Remmers, Elaine F., Goldbach-Mansky, Raphaela, Gahl, William A., O’Shea, John J., Milner, Joshua D., Lewis, Nathan E., Chang, Johanna, Kastner, Daniel L., Torok, Kathryn, Oda, Hirotsugu, Putnam, Christopher D., Broderick, Lori

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Case report: Novel variants in RELA associated with familial Behcet's-like disease von An, Jason W, Pimpale-Chavan, Pallavi, Stone, Deborah L, Bandeira, Marcia, Dedeoglu, Fatma, Lo, Jeffrey, Bohnsack, John, Rosenzweig, Sofia, Schnappauf, Oskar, Dissanayake, Dilan, Hiraki, Linda T, Kastner, Daniel L, Pelajo, Christina, Laxer, Ronald M, Aksentijevich, Ivona

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Is Anti-NXP2 Autoantibody a Risk Factor for Calcinosis and Poor Outcome in Juvenile Dermatomyositis Patients? Case Series von Toplak, Natasa, Pimpale Chavan, Pallavi, Rosina, Silvia, Dallos, Tomas, Rotem Semo, Oz, Aguiar, Cassyanne L, Khubchandani, Raju, Ravelli, Angelo, Patwardhan, Anjali

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Human TBK1 deficiency leads to autoinflammation driven by TNF-induced cell death von Taft, Justin, Markson, Michael, Legarda, Diana, Patel, Roosheel, Chan, Mark, Malle, Louise, Richardson, Ashley, Gruber, Conor, Martín-Fernández, Marta, Mancini, Grazia M.S., van Laar, Jan A.M., van Pelt, Philomine, Buta, Sofija, Wokke, Beatrijs H.A., Sabli, Ira K.D., Sancho-Shimizu, Vanessa, Chavan, Pallavi Pimpale, Schnappauf, Oskar, Khubchandani, Raju, Cüceoğlu, Müşerref Kasap, Özen, Seza, Kastner, Daniel L., Ting, Adrian T., Aksentijevich, Ivona, Hollink, Iris H.I. M., Bogunovic, Dusan

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Deficiency of Adenosine Deaminase 2 (DADA2): One Disease, Several Faces von Pimpale Chavan, Pallavi, Ramadoss, Divya, Khan, Archana, Lee, Pui Y., Khubchandani, Raju

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Deficiency of Adenosine Deaminase 2 in Adults and Children: Experience From India von Sharma, Aman, Naidu, GSRSNK, Sharma, Vikas, Jha, Saket, Dhooria, Aaadhar, Dhir, Varun, Bhatia, Prateek, Sharma, Vishal, Bhattad, Sagar, Chengappa, K. G., Gupta, Vikas, Misra, Durga Prasanna, Chavan, Pallavi Pimpale, Malaviya, Sourabh, Dudam, Rajkiran, Sharma, Banwari, Kumar, Sathish, Bhojwani, Rajesh, Gupta, Pankaj, Agarwal, Vikas, Sharma, Kusum, Singhal, Manphool, Rathi, Manish, Nada, Ritambhra, Minz, Ranjana W., Chaturvedi, Ved, Aggarwal, Amita, Handa, Rohini, Grossi, Alice, Gattorno, Marco, Huang, Zhengping, Wang, Jun, Jois, Ramesh, Negi, V. S., Khubchandani, Raju, Jain, Sanjay, Arostegui, Juan I., Chambers, Eugene P., Hershfield, Michael S., Aksentijevich, Ivona, Zhou, Qing, Lee, Pui Y.

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Development and initial validation of a composite disease activity score for systemic juvenile idiopathic arthritis von Tibaldi, Jessica, Pistorio, Angela, Aldera, Elena, Puzone, Laura, El Miedany, Yasser, Pal, Priyankar, Giri, Prabhas Prasun, De, Hriday, Khubchandani, Raju, Chavan, Pallavi Pimpale, Vilaiyuk, Soamarat, Lerkvaleekul, Butsabong, Yamsuwan, Jutamas, Sabui, Tapas K, Datta, Pragati, Pardeo, Manuela, Bracaglia, Claudia, Sawhney, Sujata, Mittal, Sumidha, Hassan, Waleed A, Elderiny, Ghada Farouk, Abu-Zaid, Mohammed Hassan, Eissa, Mervat, Sztajnbok, Flavio, das Neves Sztajnbok, Fernanda C, Russo, Ricardo, Katsicas, María Martha, Cimaz, Rolando, Marrani, Edoardo, Alexeeva, Ekaterina, Dvoryakovskaya, Tatyana M, Alsuweiti, Motasem O, Alzyoud, Ra'ed M, Kostik, Mikhail, Chikova, Irina, Minoia, Francesca, Filocamo, Giovanni, Farag, Yomna, Lotfy, Hala, Nasef, Samah Ismail, Al-Mayouf, Sulaiman M, Maggio, Maria Cristina, Magalhaes, Claudia Saad, Gallizzi, Romina, Conti, Giovanni, Shimizu, Masaki, Civino, Adele, Felici, Enrico, Giancane, Gabriella, Ruperto, Nicolino, Consolaro, Alessandro, Ravelli, Angelo

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Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation von Triaille, Clement, Rao, Neha Mohan, Rice, Gillian I, Seabra, Luis, Sutherland, Fraser J.H, Bondet, Vincent, Duffy, Darragh, Gennery, Andrew R, Fournier, Benjamin, Bader-Meunier, Brigitte, Troedson, Christopher, Cleary, Gavin, Buso, Helena, Dalby-Payne, Jacqueline, Ranade, Prajakta, Jansen, Katrien, De Somer, Lien, Fremond, Marie-Louise, Chavan, Pallavi Pimpale, Wong, Melanie, Dale, Russell C, Wouters, Carine, Quartier, Pierre, Khubchandani, Raju, Crow, Yanick J

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Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency von Oda, Hirotsugu, Manthiram, Kalpana, Chavan, Pallavi Pimpale, Rieser, Eva, Veli, Önay, Kaya, Öykü, Rauch, Charles, Nakabo, Shuichiro, Kuehn, Hye Sun, Swart, Mariël, Wang, Yanli, Çelik, Nisa Ilgim, Molitor, Anne, Ziaee, Vahid, Movahedi, Nasim, Shahrooei, Mohammad, Parvaneh, Nima, Alipour-olyei, Nasrin, Carapito, Raphael, Xu, Qin, Preite, Silvia, Beck, David B., Chae, Jae Jin, Nehrebecky, Michele, Ombrello, Amanda K., Hoffmann, Patrycja, Romeo, Tina, Deuitch, Natalie T., Matthíasardóttir, Brynja, Mullikin, James, Komarow, Hirsh, Stoddard, Jennifer, Niemela, Julie, Dobbs, Kerry, Sweeney, Colin L., Anderton, Holly, Lawlor, Kate E., Yoshitomi, Hiroyuki, Yang, Dan, Boehm, Manfred, Davis, Jeremy, Mudd, Pamela, Randazzo, Davide, Tsai, Wanxia Li, Gadina, Massimo, Kaplan, Mariana J., Toguchida, Junya, Mayer, Christian T., Rosenzweig, Sergio D., Notarangelo, Luigi D., Iwai, Kazuhiro, Silke, John, Schwartzberg, Pamela L., Boisson, Bertrand, Casanova, Jean-Laurent, Bahram, Seiamak, Rao, Anand Prahalad, Peltzer, Nieves, Walczak, Henning, Lalaoui, Najoua, Aksentijevich, Ivona, Kastner, Daniel L.

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Steroid-dependent Kimura Disease in a Child Treated with Cetirizine and Montelukast von Chavan, Pallavi Pimpale, Khubchandani, S. R., Khubchandani, R. P.

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Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation von Triaille, Clément, Rao, Neha Mohan, Rice, Gillian I., Seabra, Luis, Sutherland, Fraser J. H., Bondet, Vincent, Duffy, Darragh, Gennery, Andrew R., Fournier, Benjamin, Bader-Meunier, Brigitte, Troedson, Christopher, Cleary, Gavin, Buso, Helena, Dalby-Payne, Jacqueline, Ranade, Prajakta, Jansen, Katrien, De Somer, Lien, Frémond, Marie-Louise, Chavan, Pallavi Pimpale, Wong, Melanie, Dale, Russell C., Wouters, Carine, Quartier, Pierre, Khubchandani, Raju, Crow, Yanick J.

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Clinical features, severity and outcome of acute pancreatitis in systemic lupus erythematosus von Muhammed, Hafis, Jain, Avinash, Irfan, Mohammad, Charles, Sheba, Dwivedi, Preksha, Chavan, Pallavi Pimpale, Khubchandani, Raju, Sharma, Amit, Phatak, Sanat, Shukla, Anuj N., Shah, Ripal, Subramanian, N., Pandya, Sapan C., Singh, Yogesh Preet, Chengappa, K. G., Thabah, Molly, Rajasekhar, Liza, Shobha, Vineeta, Negi, V. S., Dhir, Varun, Sharma, Aman, Misra, Ramnath, Aggarwal, Amita

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Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID) von Nair, Sona B., Chavan, Pallavi Pimpale, Athalye, Arundhati S., Aksentijevich, Ivona, Khubchandani, Raju P.

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Wide variation in glucocorticoid dosing in paediatric ANCA-associated vasculitis with renal disease: a paediatric vasculitis initiative study von Chen, Audrea, Mammen, Cherry, Guzman, Jaime, Al-Abadi, Eslam, Benseler, Susanne M, Berard, Roberta A, Gerstbacher, Dana, Heshin-Bekenstein, Merav, Kim, Susan, Klein-Gitelman, Marisa, Chavan, Pallavi Pimpale, James, Karen E, Martin, Neil, McErlane, Flora, Myrup, Charlotte, Noone, Damien G, Raghuram, Jyothi, Shenoi, Susan, Sivaraman, Vidya, Tanner, Tamara, Yeung, Rae S M, Cabral, David A, Morishita, Kimberly A

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Case report: Novel variants in RELA associated with familial Behcet's-like disease von An, Jason W, Pimpale-Chavan, Pallavi, Stone, Deborah L, Bandeira, Marcia, Dedeoglu, Fatma, Lo, Jeffrey, Bohnsack, John, Rosenzweig, Sofia, Schnappauf, Oskar, Dissanayake, Dilan, Hiraki, Linda T, Kastner, Daniel L, Pelajo, Christina, Laxer, Ronald M, Aksentijevich, Ivona

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Is Anti-NXP2 Autoantibody a Risk Factor for Calcinosis and Poor Outcome in Juvenile Dermatomyositis Patients? Case Series von Toplak, Natasa, Pimpale Chavan, Pallavi, Rosina, Silvia, Dallos, Tomas, Rotem Semo, Oz, Aguiar, Cassyanne L, Khubchandani, Raju, Ravelli, Angelo, Patwardhan, Anjali

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